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临床试验/NCT04803851
NCT04803851招募中1 期

Anlotinib Plus Anti-PD-1 Antibody AK105 as Third or More-line Therapy for Advanced Pancreatic Cancer: a Prospective, Single-arm, Open-label, Pilot Study

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2021年5月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
29
试验地点
1
主要终点
Disease control rate (DCR) based on RECIST v. 1 1

研究概览

简要总结

This study was designed to explore the clinical efficacy of Anlotinib combined with Anti-PD-1 antibody AK105 in the treatment of third- and above -line advanced pancreatic cancer patients, in order to find a better therapy strategy for pancreatic cancer patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • locally advanced or metastatic pancreatic cancer (PC),
  • histologically or cytologically proven diagnosis of adenocarcinoma or adenosquamous carcinoma,
  • failed to second-line chemotherapy for PC,
  • 18-75 years of age,
  • an Eastern Cooperative Oncology Group performance status score of 0 to 1,
  • adequate organ functions

排除标准

  • had received PD 1 /CTLA 4 antibody treatment
  • had received anti-VEGFR inhibitors or antibodies

研究组 & 干预措施

Treatment group

Experimental

Anlotinib plus AK105

干预措施: Anlotinib plus AK105 (Drug)

结局指标

主要结局

Disease control rate (DCR) based on RECIST v. 1 1

时间窗: 6 weeks

Disease control rate (DCR) based on RECIST v. 1 1 by investigators

次要结局

  • Objective response rate (ORR) based on RECIST V. 1.1(6 weeks)
  • Progression free survival (PFS) measured from the date of anlotinib plus AK105 initiation to the time of progression(6 weeks)
  • Overall survival (OS) measured from the date of anlotinib plus AK105 initiation to the time of death of any cause(6 weeks)
  • Number of participants with treatment-related adverse events as assessed by CTCAE v4.0(6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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